Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | calcium-activated potassium channel | 0.1269 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0636 | 0.3965 | 0.0935 |
Schistosoma mansoni | hypothetical protein | 0.1269 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1269 | 1 | 1 |
Trypanosoma cruzi | lanosterol synthase, putative | 0.0317 | 0.0918 | 0.5 |
Trypanosoma cruzi | lanosterol synthase, putative | 0.0317 | 0.0918 | 0.5 |
Mycobacterium tuberculosis | Halimadienyl diphosphate synthase | 0.022 | 0 | 0.5 |
Leishmania major | lanosterol synthase, putative | 0.0287 | 0.0637 | 0.5 |
Trypanosoma brucei | lanosterol synthase | 0.0317 | 0.0918 | 0.5 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.1269 | 1 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
ED50 (functional) | = 50000 nM | In vitro activity of the compound to inhibit MCP-1-induced leukocyte migration of THP-1 cells | ChEMBL. | 15689171 |
ED50 (functional) | = 50000 nM | In vitro activity of the compound to inhibit MCP-1-induced leukocyte migration of THP-1 cells | ChEMBL. | 15689171 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.